Author:
Sela Ilan,Yakovlev Lena,Becker Cohen Michal,Elbaz Moran,Yanay Nurit,Ben Shlomo Uri,Yotvat Hagit,Fellig Yakov,Argov Zohar,Mitrani-Rosenbaum Stella
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology,Molecular Medicine
Reference30 articles.
1. Argov, Z., Eisenberg, I., & Mitrani-Rosenbaum, S. (1998). Genetics of inclusion body myopathies. Current Opinion in Rheumatology, 10, 543–547.
2. Argov, Z., & Mitrani-Rosenbaum, S. (2008). The hereditary inclusion body myopathy enigma and its future therapy. Neurotherapeutics, 5, 633–637.
3. Argov, Z., & Yarom, R. (1984). ‘Rimmed vacuole myopathy’ sparing the quadriceps: A unique disorder in Iranian Jews. Journal of the Neurological Sciences, 64, 33–43.
4. Broccolini, A., Gidaro, T., Morosetti, R., Sancricca, C., & Mirabella, M. (2011). Hereditary inclusion-body myopathy with sparing of the quadriceps: The many tiles of an incomplete puzzle. Acta Myologica, 30, 91–95.
5. Broccolini, A., Gliubizzi, C., Pavoni, E., et al. (2005). Alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy. Neuromuscular Disorders, 15, 177–184.
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